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Artykuły w czasopismach na temat „In vivo assay”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 10 lutego 2022

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1

Hayashi, Makoto, James T. MacGregor, David G. Gatehouse, et al. "In vivo erythrocyte micronucleus assay." Mutation Research/Genetic Toxicology and Environmental Mutagenesis 627, no. 1 (2007): 10–30. http://dx.doi.org/10.1016/j.mrgentox.2006.08.010.

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2

Kim, So-Jung, Young-Jae Chung, and Taek-Kyun Lee. "In vivo Comet Assay on Flounder and Clam Exposed to BaP and TBT." Ocean and Polar Research 33, no. 2 (2011): 127–33. http://dx.doi.org/10.4217/opr.2011.33.2.127.

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3

Matute, Alexis, Jessica Tabart, Jean-Paul Cheramy-Bien, et al. "Ex Vivo Antioxidant Capacities of Fruit and Vegetable Juices. Potential In Vivo Extrapolation." Antioxidants 10, no. 5 (2021): 770. http://dx.doi.org/10.3390/antiox10050770.

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Background: In support of claims that their products have antioxidant properties, the food industry and dietary supplement manufacturers rely solely on the in vitro determination of the ORAC (oxygen radical antioxidant capacity) value, despite its acknowledged lack of any in vivo relevance. It thus appears necessary to use tests exploiting biological materials (blood, white blood cells) capable of producing physiological free radicals, in order to evaluate more adequately the antioxidant capacities of foods such as fruit and vegetable juices. Materials: Two approaches to assessing the antioxid

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4

Simpson, David M., Edward W. Stoller, and Loyd M. Wax. "An in vivo Acetolactate Synthase Assay." Weed Technology 9, no. 1 (1995): 17–22. http://dx.doi.org/10.1017/s0890037x00022879.

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A method was developed and tested for in vivo assay of acetolactate synthase (ALS). The method used foliar application of 1,1-cyclopropanedicarboxylic acid (CPCA) to inhibit ketol-acid reductoisomerase, the enzyme immediately following ALS in biosynthesis of branched-chain amino acids, thereby causing accumulation of acetolactate. Since the amount of acetolactate accumulation is a function of carbon flux through ALS, quantification of acetolactate accumulation determined ALS activity. Accumulation of acetolactate in soybean leaves resulted from CPCA rates as low as 15 g/ha and occurred within

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5

Hayashi, Makoto, Raymond R. Tice, James T. MacGregor, et al. "In vivo rodent erythrocyte micronucleus assay." Mutation Research/Environmental Mutagenesis and Related Subjects 312, no. 3 (1994): 293–304. http://dx.doi.org/10.1016/0165-1161(94)90039-6.

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6

Spach, Colette, and Roland Motta. "In vivo eight-day ‘MLR’ assay." Journal of Immunological Methods 97, no. 2 (1987): 259–62. http://dx.doi.org/10.1016/0022-1759(87)90468-6.

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7

Uccellini, Melissa B., Sadaf Aslam, Sean T. H. Liu, Fahmida Alam, and Adolfo García-Sastre. "Development of a Macrophage-Based ADCC Assay." Vaccines 9, no. 6 (2021): 660. http://dx.doi.org/10.3390/vaccines9060660.

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Fc-dependent effector functions are an important determinant of the in vivo potency of therapeutic antibodies. Effector function is determined by the combination of FcRs bound by the antibody and the cell expressing the relevant FcRs, leading to antibody-dependent cellular cytotoxicity (ADCC). A number of ADCC assays have been developed; however, they suffer from limitations in terms of throughput, reproducibility, and in vivo relevance. Existing assays measure NK cell-mediated ADCC activity; however, studies suggest that macrophages mediate the effector function of many antibodies in vivo. He

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8

Hosking, Laine, Christine Czakjo, and Sharon Choo. "Implementation of an ex vivo TH17 assay." Pathology 49 (February 2017): S43. http://dx.doi.org/10.1016/j.pathol.2016.12.102.

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9

Bertaccini, Alessandro, Catia Giovannini, Domenico Viola, et al. "Telomerase assay from ex vivo prostate biopsies." European Urology Supplements 1, no. 1 (2002): 119. http://dx.doi.org/10.1016/s1569-9056(02)80461-4.

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10

Tang, De-chu, Adi F. Gazdar, and David P. Carbone. "In vivo cytotoxicity assay for assessing immunity." Journal of Immunological Methods 189, no. 2 (1996): 173–82. http://dx.doi.org/10.1016/0022-1759(95)00234-0.

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11

Simon, P., H. Ottenwälder, and H. M. Bolt. "Vinyl acetate: DNA-binding assay in vivo." Toxicology Letters 27, no. 1-3 (1985): 115–20. http://dx.doi.org/10.1016/0378-4274(85)90128-6.

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12

Russell, Bruce, Rossarin Suwanarusk, Céline Borlon, et al. "A reliable ex vivo invasion assay of human reticulocytes by Plasmodium vivax." Blood 118, no. 13 (2011): e74-e81. http://dx.doi.org/10.1182/blood-2011-04-348748.

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AbstractCurrently, there are no reliable RBC invasion assays to guide the discovery of vaccines against Plasmodium vivax, the most prevalent malaria parasite in Asia and South America. Here we describe a protocol for an ex vivo P vivax invasion assay that can be easily deployed in laboratories located in endemic countries. The assay is based on mixing enriched cord blood reticulocytes with matured, trypsin-treated P vivax schizonts concentrated from clinical isolates. The reliability of this assay was demonstrated using a large panel of P vivax isolates freshly collected from patients in Thail

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13

Symonds, Jennifer M., Tomohiro Fujita, Shouhei Aoki, Kazuma Shiota та Claire L. Kruger. "Toxicological assessment of β-galactosidase shows no adverse effects in vivo and in vitro". Toxicology Research and Application 4 (1 січня 2020): 239784732090877. http://dx.doi.org/10.1177/2397847320908776.

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A safety assessment for β-galactosidase derived from Aspergillus oryzae (GODO-FAL) was performed. The test article was a concentrated, purified β-galactosidase diluted in glycerin and water with an activity of 10,000 U/mL. A series of genotoxicology tests including micronucleus assay, chromosome aberration assay, and reverse mutagenesis (Ames) assay confirmed that GODO-FAL was not clastogenic or mutagenic at any of the concentrations used, up to 2000 µg/mL for the chromosome aberration assay and 5000 mg per plate in the Ames assay. GODO-FAL was not toxic in acute, repeated oral toxicity, and s

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14

Unseld, Matthias, Johannes M. Breuss, Clemens Pausz, et al. "In vivo Tube Assay: An Optimised Protocol of the Directed in vivo Angiogenesis Assay by Implementing Immunohistochemistry." Journal of Vascular Research 52, no. 2 (2015): 116–26. http://dx.doi.org/10.1159/000434751.

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15

Brattig, N. W., C. Timmann, R. S. Abraha, B. Lepping, B. Muller-Myhsok, and R. D. Horstmann. "Relevance of ex vivo blood lymphocyte assay for in vivo lymphocyte function." Clinical and Experimental Immunology 139, no. 1 (2005): 127–31. http://dx.doi.org/10.1111/j.1365-2249.2005.02667.x.

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16

Romli, Firdaus, Nadiah Abu, Faten A. Khorshid, et al. "The Growth Inhibitory Potential and Antimetastatic Effect of Camel Urine on Breast Cancer Cells In Vitro and In Vivo." Integrative Cancer Therapies 16, no. 4 (2016): 540–55. http://dx.doi.org/10.1177/1534735416656051.

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Although it may sound unpleasant, camel urine has been consumed extensively for years in the Middle East as it is believed to be able to treat a wide range of diseases such as fever, cold, or even cancer. People usually take it by mixing small drops with camel milk or take it directly. The project aims to study the effects of camel urine in inhibiting the growth potential and metastatic ability of 4T1 cancer cell line in vitro and in vivo. Based on the MTT result, the cytotoxicity of camel urine against 4T1 cell was established, and it was dose-dependent. Additionally, the antimetastatic poten

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17

Yesildal, F., FN Aydin, S. Deveci, et al. "Aspartame induces angiogenesis in vitro and in vivo models." Human & Experimental Toxicology 34, no. 3 (2014): 260–65. http://dx.doi.org/10.1177/0960327114537535.

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Angiogenesis is the process of generating new blood vessels from preexisting vessels and is considered essential in many pathological conditions. The purpose of the present study is to evaluate the effect of aspartame on angiogenesis in vivo chick chorioallantoic membrane (CAM) and wound-healing models as well as in vitro 2,3-bis-2 H-tetrazolium-5-carboxanilide (XTT) and tube formation assays. In CAM assay, aspartame increased angiogenesis in a concentration-dependent manner. Compared with the control group, aspartame has significantly increased vessel proliferation ( p < 0.001). In additio

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18

Hao, Nan, Adrienne E. Sullivan, Keith E. Shearwin, and Ian B. Dodd. "The loopometer: a quantitative in vivo assay for DNA-looping proteins." Nucleic Acids Research 49, no. 7 (2021): e39-e39. http://dx.doi.org/10.1093/nar/gkaa1284.

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Abstract Proteins that can bring together separate DNA sites, either on the same or on different DNA molecules, are critical for a variety of DNA-based processes. However, there are no general and technically simple assays to detect proteins capable of DNA looping in vivo nor to quantitate their in vivo looping efficiency. Here, we develop a quantitative in vivo assay for DNA-looping proteins in Escherichia coli that requires only basic DNA cloning techniques and a LacZ assay. The assay is based on loop assistance, where two binding sites for the candidate looping protein are inserted internal

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19

Miura, Daishiro. "The In Vivo Pig-a Gene Mutation Assay." Genes and Environment 36, no. 4 (2014): 169–73. http://dx.doi.org/10.3123/jemsge.2014.027.

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20

Parng, Chuenlei, Christopher Ton, Ying-Xin Lin, Nicole Marie Roy, and Patricia McGrath. "A zebrafish assay for identifying neuroprotectants in vivo." Neurotoxicology and Teratology 28, no. 4 (2006): 509–16. http://dx.doi.org/10.1016/j.ntt.2006.04.003.

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21

Kim, Byung Soo, Myung-Haing Cho, and Hyun Jung Kim. "Statistical analysis of in vivo rodent micronucleus assay." Mutation Research/Genetic Toxicology and Environmental Mutagenesis 469, no. 2 (2000): 233–41. http://dx.doi.org/10.1016/s1383-5718(00)00085-1.

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22

Schuster, Sascha, Markus Enzelberger, Harald Trauthwein, Rolf D. Schmid, and Vlada B. Urlacher. "pHluorin-Based in Vivo Assay for Hydrolase Screening." Analytical Chemistry 77, no. 9 (2005): 2727–32. http://dx.doi.org/10.1021/ac0486692.

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23

Miraucourt, Lois, Michael Accardi, Hai Huang, and Simon Authier. "Proof of concept comprehensive ex vivo neurological assay." Journal of Pharmacological and Toxicological Methods 99 (September 2019): 106595. http://dx.doi.org/10.1016/j.vascn.2019.05.137.

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24

Lee, Wenjau, Chi-Wei Kan, Chung-Kai Su, Kataaki Okubo, and Yoshitaka Nagahama. "Detecting xenoestrogens with an in vivo assay system." Toxicology Letters 211 (June 2012): S49—S50. http://dx.doi.org/10.1016/j.toxlet.2012.03.199.

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25

Goldberg, M. T., and P. Chidiac. "An in vivo assay for small intestine genotoxicity." Mutation Research/Environmental Mutagenesis and Related Subjects 164, no. 4 (1986): 209–15. http://dx.doi.org/10.1016/0165-1161(86)90055-5.

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26

Hothorn, Ludwig A., and Daniel Gerhard. "Statistical evaluation of the in vivo micronucleus assay." Archives of Toxicology 83, no. 6 (2008): 625–34. http://dx.doi.org/10.1007/s00204-008-0393-8.

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27

Dasgupta, Amitava, Edward Kang, Margaret Olsen, Jeffrey K. Actor, and Pradip Datta. "Interference of Asian, American, and Indian (Ashwagandha) Ginsengs in Serum Digoxin Measurements by a Fluorescence Polarization Immunoassay Can Be Minimized by Using a New Enzyme-Linked Chemiluminescent Immunosorbent or Turbidimetric Assay." Archives of Pathology & Laboratory Medicine 131, no. 4 (2007): 619–21. http://dx.doi.org/10.5858/2007-131-619-ioaaai.

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Abstract Context.—Ginsengs are widely used by the general population. These herbs interfere with serum digoxin measurement using the fluorescence polarization immunoassay. Objective.—To assess potential interference of different ginsengs (Asian, American, and Indian, also known as Ashwagandha) in vitro and in vivo in a mouse model by using a new enzyme-linked chemiluminescent immunosorbent digoxin assay and an existing turbidimetric assay. Comparisons were made with the fluorescence polarization immunoassay. Design.—Aliquots of drug-free serum pools were supplemented with ginseng and apparent

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28

Meneses, J. O., M. V. S. do Couto, N. C. Sousa, et al. "Efficacy of Ocimum gratissimum essential oil against the monogenean Cichlidogyrus tilapiae gill parasite of Nile tilapia." Arquivo Brasileiro de Medicina Veterinária e Zootecnia 70, no. 2 (2018): 497–504. http://dx.doi.org/10.1590/1678-4162-9667.

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ABSTRACT The phythotherapy is an alternative to use of chemotherapeutical agents against monogenean infection. This study evaluated the anthelmintic activity of essential oil Ocimum gratissimum against monogenean Cichlidogyrus tilapiae as well as its acute toxicity in tilapia juveniles. The mean lethal concentration (LC50) and different concentrations of the essential oil, both in vitro and in vivo assays (short and long-term baths) were assessed. The LC50 was 40.70mg.L-1 and in the in vitro assay this concentration showed 80% efficacy at the last two hours and in the in vivo assay 65.87% effi

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29

Wegulo, Stephen N., and Miguel Vilchez. "Evaluation of Lisianthus Cultivars for Resistance to Botrytis cinerea." Plant Disease 91, no. 8 (2007): 997–1001. http://dx.doi.org/10.1094/pdis-91-8-0997.

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Lisianthus (Eustoma grandiflorum) is a high-value cut flower. However, major yield losses often result from gray mold caused by Botrytis cinerea. Various techniques were used to evaluate 12 lisianthus cultivars for resistance B. cinerea. Disease evaluations from detached leaf, leaf disc, cut stem, and in vivo growth chamber stem (GC) assays were correlated with those from an in vivo greenhouse stem (GH) assay, in which commercial greenhouse production of lisianthus was simulated. In all assays, stems or leaves were wounded before inoculation with spores or mycelia of B. cinerea. There was a si

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30

Lee, Sun Young, Hee Jung Lee, Heejin Lee, Shukho Kim, Eun Hee Cho, and Heon Man Lim. "In Vivo Assay of Protein-Protein Interactions in Hin-Mediated DNA Inversion." Journal of Bacteriology 180, no. 22 (1998): 5954–60. http://dx.doi.org/10.1128/jb.180.22.5954-5960.1998.

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ABSTRACT In order to form the catalytic nucleoprotein complex called the invertasome in the Hin-mediated DNA inversion reaction, interactions of the DNA-binding proteins Hin and Fis are required. Assays for these protein-protein interactions have been exploited with protein cross-linkers in vitro. In this study, an in vivo assay system that probes protein-protein interactions was developed. The formation of a DNA loop generated by protein interactions resulted in transcriptional repression of an artificially designed operon, which in turn increased the chance of survival of Escherichia colihos

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31

Lee, Eun-Gyung, and Maxine L. Linial. "Yeast Three-Hybrid Screening of Rous Sarcoma Virus Mutants with Randomly Mutagenized Minimal Packaging Signals Reveals Regions Important for Gag Interactions." Journal of Virology 74, no. 19 (2000): 9167–74. http://dx.doi.org/10.1128/jvi.74.19.9167-9174.2000.

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ABSTRACT We previously showed that the yeast three-hybrid system provides a genetic assay of both RNA and protein components for avian retroviral RNA encapsidation. In the current study, we used this assay to precisely define cis-acting determinants involved in avian leukosis sarcoma virus packaging RNA binding to Gag protein. In vivo screening of Rous sarcoma virus mutants was performed with randomly mutated minimal packaging sequences (MΨ) made using PCR amplification after cotransformation with GagΔPR protein into yeast cells. Colonies with low β-galactosidase activity were analyzed to loca

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32

Lee, Keyong Ho, and Ki Hyeong Rhee. "Correlative Effect between in vivo Hollow Fiber Assay and Xenografts Assay in Drug Screening." Cancer Research and Treatment 37, no. 3 (2005): 196. http://dx.doi.org/10.4143/crt.2005.37.3.196.

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Rainbolt, Curtis R., Donald C. Thill, Robert S. Zemetra, and Dale L. Shaner. "Imidazolinone-Resistant Wheat Acetolactate Synthase In Vivo Response to Imazamox." Weed Technology 19, no. 3 (2005): 539–48. http://dx.doi.org/10.1614/wt-03-215r1.1.

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Several experiments were conducted to evaluate the utility of an in vivo acetolactate synthase (ALS) assay for comparing sensitivity to imazamox among imidazolinone-resistant wheat cultivars/lines. Ten single-gene imidazolinone-resistant winter wheat cultivars/lines, one two-gene and four single-gene imidazolinone-resistant spring wheat cultivars/lines, and three pairs of heterozygous and homozygous imidazolinone-resistant winter wheat lines were evaluated in the assay experiments. Additionally, a dose-response assay was conducted to evaluate the tolerance of several imidazolinone-resistant wh

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34

Liu, Lili, Zhiying Xu, Binbin Yu, Li Tao, and Ying Cao. "Berbamine Inhibits Cell Proliferation and Migration and Induces Cell Death of Lung Cancer Cells via Regulating c-Maf, PI3K/Akt, and MDM2-P53 Pathways." Evidence-Based Complementary and Alternative Medicine 2021 (July 8, 2021): 1–20. http://dx.doi.org/10.1155/2021/5517143.

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Berbamine (BBM) is a natural product isolated from Berberis amurensis Rupr. We investigated the influence of BBM on the cell viability, proliferation, and migration of lung cancer cells and explored the possible mechanisms. The cell viability and proliferation of lung cancer cells were evaluated by MTT assay, EdU assay, and colony formation assay. Migration and invasion abilities of cancer cells were determined through wound scratch assay and Transwell assay. Cell death was evaluated by cell death staining assay and ELISA. The expressions of proteins were evaluated using western blot assay. A

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35

Amano, Yuto, Hiroshi Honda, Yuko Nukada, et al. "Safety Pharmacological Evaluation of the Coffee Component, Caffeoylquinic Acid, and Its Metabolites, Using Ex Vivo and In Vitro Profiling Assays." Pharmaceuticals 12, no. 3 (2019): 110. http://dx.doi.org/10.3390/ph12030110.

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Although coffee components have gained interest for use as pharmaceuticals, little is known about their safety pharmacological effects. Hence, we aimed to evaluate the safety pharmacological effects of a chlorogenic acid (CGA)-related compound contained in coffee, 5-O-caffeoylquinic acid (5-CQA), and its metabolites, 5-O-feruloylquinic acid (5-FQA), caffeic acid (CA), and ferulic acid (FA). Langendorff perfused heart assay, electrophysiological assay of acute rat hippocampal slices, and in vitro Magnus assay of gastrointestinal tracts were conducted at 1–100 µM. Moreover, in vitro profiling as

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36

Toyoizumi, Tomoyasu, Ryo Ohta, Kumiko Kawakami, et al. "Usefulness of combined in vivo skin comet assay and in vivo skin micronucleus test." Mutation Research/Genetic Toxicology and Environmental Mutagenesis 743, no. 1-2 (2012): 42–51. http://dx.doi.org/10.1016/j.mrgentox.2011.12.020.

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GOMEZ‐TREVINO, M., H. BOUREAU, T. KARJALAINEN, and P. BOURLIOUX. "Clostridium difficile Adherence to Mucus: Results of an in vivo and ex vivo Assay." Microbial Ecology in Health and Disease 9, no. 6 (1996): 329–34. http://dx.doi.org/10.1002/(sici)1234-987x(199611)9:6<329::aid-meh329>3.3.co;2-c.

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Rashid, S. Z., and M. Kyo. "IN VIVO FUNCTIONAL ASSAY OF WUS ORTHOLOG IN TOBACCO." Acta Horticulturae, no. 829 (June 2009): 161–66. http://dx.doi.org/10.17660/actahortic.2009.829.23.

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Hayashi, Makoto. "The in vivo rodent erythrocyte micronucleus assay (automated scoring)." Toxicology 226, no. 1 (2006): 34–35. http://dx.doi.org/10.1016/j.tox.2006.05.053.

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Ly, Suw Young, Kyung Lee, Jung Ki Baek, Ung June Kang, and Seungjun Lee. "Electro Diagnostic Nerve Feeling Assay in In-Vivo Muscles." KOREA SCIENCE & ART FORUM 36 (December 31, 2018): 247–54. http://dx.doi.org/10.17548/ksaf.2018.12.30.247.

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Api, A. M., and R. Gudi. "An in vivo mouse micronucleus assay on musk ketone." Mutation Research/Genetic Toxicology and Environmental Mutagenesis 464, no. 2 (2000): 263–67. http://dx.doi.org/10.1016/s1383-5718(99)00202-8.

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Sarnaizul, Erdenebaatar, Gereltu Borjihan, and Sun Zhaorigetu. "The preparation and antihyperlipidaemic assay of piperlonguminine in vivo." Phytochemistry Letters 6, no. 1 (2013): 101–5. http://dx.doi.org/10.1016/j.phytol.2012.12.002.

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Kim, Duk Yoon, and Je Chul Lee. "Adherence Assay of UropathogenicEscherichia coliIn Vivo and In Vitro." Urogenital Tract Infection 12, no. 3 (2017): 122. http://dx.doi.org/10.14777/uti.2017.12.3.122.

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44

Hartmann, A. "Recommendations for conducting the in vivo alkaline Comet assay." Mutagenesis 18, no. 1 (2003): 45–51. http://dx.doi.org/10.1093/mutage/18.1.45.

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Corkery, Dale P., Graham Dellaire, and Jason N. Berman. "Leukaemia xenotransplantation in zebrafish - chemotherapy response assay in vivo." British Journal of Haematology 153, no. 6 (2011): 786–89. http://dx.doi.org/10.1111/j.1365-2141.2011.08661.x.

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46

Richardson-Harman, Nicola, Robert Parody, Peter Anton, et al. "Analytical Advances in the Ex Vivo Challenge Efficacy Assay." AIDS Research and Human Retroviruses 33, no. 4 (2017): 395–403. http://dx.doi.org/10.1089/aid.2016.0073.

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Maxwell, Karen L., Anthony K. Mittermaier, Julie D. Forman-Kay, and Alan R. Davidson. "A simple in vivo assay for increased protein solubility." Protein Science 8, no. 9 (1999): 1908–11. http://dx.doi.org/10.1110/ps.8.9.1908.

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48

Rizzo, Larissa Y., Susanne K. Golombek, Marianne E. Mertens, et al. "In vivo nanotoxicity testing using the zebrafish embryo assay." Journal of Materials Chemistry B 1, no. 32 (2013): 3918. http://dx.doi.org/10.1039/c3tb20528b.

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Butler, Scott L., Mark S. T. Hansen, and Frederic D. Bushman. "A quantitative assay for HIV DNA integration in vivo." Nature Medicine 7, no. 5 (2001): 631–34. http://dx.doi.org/10.1038/87979.

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Rezzola, Sara, Mirella Belleri, Domenico Ribatti, Ciro Costagliola, Marco Presta, and Francesco Semeraro. "A novel ex vivo murine retina angiogenesis (EMRA) assay." Experimental Eye Research 112 (July 2013): 51–56. http://dx.doi.org/10.1016/j.exer.2013.04.014.

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